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Methanol → Methyl 3-bromo-2-methoxybenzoate

HRID 1042350
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HRID 1042350 반응식
[Br:1][C:2]1[C:3]([O:11][CH3:12])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[CH3:13]O>S(=O)(=O)(O)O>[CH3:13][O:6][C:5](=[O:7])[C:4]1[CH:8]=[CH:9][CH:10]=[C:2]([Br:1])[C:3]=1[O:11][CH3:12]
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참가 물질

4

반응물 2

HCID 887MethanolHCID 2535983-Bromo-2-methoxybenzoic acid

생성물 1

HCID 46311082Methyl 3-bromo-2-methoxybenzoate

시약·촉매·용매 1

HCID 1118Sulfuric Acid촉매

실험 절차

Approximately two drops of sulfuric acid were added to a solution of 3-bromo-2-methoxy-benzoic acid (10.00 g, 43.30 mmol) in methanol and the resulting reaction mixture was refluxed for 14 hours. The reaction mixture was cooled to room temperature, and concentrated, then diluted with EtOAc. The organic layer was washed with saturated NaHCO3 (3×150 mL), H2O (2×250 mL), brine (1×250 mL) and dried over MgSO4. The crude product was purified by column chromatography using hex:EtOAc (4.5:0.5) as the eluant to give the title ester. Spectroscopic data: 1H NMR (300 MHz, CDCl3) δ 3.91 (s, 3H), 3.94 (s, 3H), 6.92 (d, J=8.79 Hz, 1H), 7.99 (dd, J=8.79 Hz, 1H), 8.24 (d, J=2.35 Hz, 1H).

후처리

  1. customthe resulting reaction mixture
  2. temperaturewas refluxed for 14 hours
  3. concentrationconcentrated
  4. additiondiluted with EtOAc
  5. washThe organic layer was washed with saturated NaHCO3 (3×150 mL), H2O (2×250 mL), brine (1×250 mL)
  6. dry with materialdried over MgSO4
  7. customThe crude product was purified by column chromatography

출처 및 근거

ORD 기록
ord-cb90c21ff234438dbb459dc727189e22
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08557853B2

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